A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563223



Internal ID22431963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13682077..13682077hg38UCSC Ensembl
chr3:13723576..13723576hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305358, nssv14305360, nssv14305359
SamplesNA19238, NA19239, NA19240
Known GenesLINC00620
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563223
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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